|Publication number||US3570476 A|
|Publication date||Mar 16, 1971|
|Filing date||Nov 18, 1968|
|Priority date||Nov 18, 1968|
|Publication number||US 3570476 A, US 3570476A, US-A-3570476, US3570476 A, US3570476A|
|Inventors||David Paul Gregg|
|Original Assignee||David Paul Gregg|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (2), Referenced by (28), Classifications (14)|
|External Links: USPTO, USPTO Assignment, Espacenet|
HL] 333 CA Inventor David Paul Gregg 1936 Ketton Ave., Los Angeles, Calif. 90025 Appl. No. 776,575
Filed Nov. 18, 1968 Patented Mar. 16, I971 MAGNETOSTRICTIVE MEDICAL INSTRUMENT 9 Claims, 5 Drawing Figs.
U.S. C1 128/24, 128/303 Int. Cl. A6lh 1/00,
A6lb 17/00 Field ol'Search 128/2, 24,
Pumped od/far! 10/716 V4/re fa (arr/fa f  References Cited UNITED STATES PATENTS 3,352,303 11/1967 Delaney 128/24 3,433,226 3/1969 Boyd 128/24X Primary Examiner-L. W. Trapp Attomey-Jessup and Beecher ABSTRACT: A medical instrument which may be inserted into an artery of a patient, and which includes a magnetostrictive element that serves to remove cholesterol or other fatty deposits from the interior wall of the artery. The term magnetostrigtjye'l as nsed herein is intended to embrace the emalenlelements, si ch as piezoelectric? and electrosmm" in which mechanical vibrations may be setup by the application of electrical energy.
50/11/101 f'a Fi/faf MAGNETOSTRICTIVE MEDICAL INSTRUMENT BACKGROUND OF THE INVENTION As is well known, the arteries are the vascular tubes which carry the blood away from the heart. The larger arteries normally have a smooth endothelial lining. The blood flow through the arteries is often impeded by the partial occlusion thereof, and this occlusion often is caused by the deposit of cholesterol or other fatty materials on the endothelial lining of the arteries. Prior to the advent of the present invention, the aforesaid deposits were usually removed from the arterial walls by inserting a catheter type of instrument and scraping the deposits from the arterial wall. This technique, however, is not entirely satisfactory, since it may dislodge particles, or damage the arterial lining.
The instrument of the present invention, as mentioned above, includes a magnetostrictive element which is inserted through an incision into the artery to be treated, and which can be moved along the interior of the artery, for example, by a stainless steel wire, or the like, which is attached to the element and which extends out through the incision. The instrument further includes, for example, a secondary winding which is wound about the magnetostrictive element. This secondary winding is excited by a high ultrasonic signal by means ofwmg inding, for example, which may be positioned externally of the patient and yet in an inductively coupled relationship with the secondary winding.
The excitation of the aforesaid secondary winding by the ultrasonic current in the primary winding, sets up high frequency ultrasonic vibrations in the magnetostrictive element. Suitable damping means may be provided at one end of the magnetostrictive element, so that when the element is moved along the interior of the artery, the ultrasonic vibrations of its other end cause the deposits on the arterial wall to be dislodged and washed away by an externally introduced solution.
BRIEF DESCRIPTION OF THE DRAWING FIG. 1 is a representation of the arm of a patient, and showing the instrument of the invention inserted into an artery for accomplishing the stated purpose of the invention;
FIG. 2 is a view of the magnetostrictive element which is included in the embodiment of the invention to be described;
FIG. 3 is the structure which is used to excite the element of FIG. 2 and which, i n the illustrated embodiment, may be positioned externally of the patient;
FIG. 4 is a representation of a second embodiment; and
FIG. 5 is a third embodiment of the invention.
DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS In the practice of the invention, insofar as the illustrated embodiment is concerned, and as shown in FIG. I, the instrument of the invention may be inserted through an incision in, for example, the arm 12 of the patient. The magnetostrictive element 14 of the instrument of the invention is inserted through the incision 10, and into the interior of an artery 16 by means, for example, of a stainless steel wire 18 which extends through a tubular catheter 19. The wire may have sufficient rigidity, so that it may be used to push the element 14 along the interior of the artery 16. The magnetostrictive element 14 may be excited in the manner to be described; or it ma c its own prima and seco oils, or ot ta.- tion means, which may be energized throughelectrical conductors in the wirelike element 18. 1
In the illustrated embodiment, and as shown in FIG. 2, the internal element 14 may be composed of a rod of magnetostrictive material, such as nickel, a ferrite formed, for example, of sintered oxides or iron, nickel, copper, or any other suitable magnetostrictive material. The rod, for example, may have a diameter of l millimeter. A damper 20 is mounted at one end of the rod 14. The damper 20 may be composed of any appropriate material, and should exhibit a relatively large mass with respect to the element 14, so that magnetostrictions set up in the element 14 result in a rapid movement of the end of the element remote from the damper 20. A biasing permanent magnet 21, formed of Alnico, ferrite or other appropriate permanent magnet material, should be interposed between the damper and the rod, as shown. In this way, the latter end of the element is caused to vibrate so as to dislodge and disperse cholesterol and other fatty deposits which have formed on the arterial wall. However, the dispersion is very fine, rather than in particles which could cause embolisms. These deposits become partially dissolved and are washed away by an externally introduced solution, introduced upstream of the point at which the rod is located.
The magnetostrictive effect is set up in the illustrated embodiment by a secondary winding 22 which is wound about the periphery of the magnetostrictive element 14 and around the permanent magnet 21, and which has its ends short circuited, so that an appreciable current flows through the winding 22 when it is excited. The winding 22 may be excited by an external primary winding assembly including, for example, a ring cope2 ving a primary winding 28 wound about it.
Thelcore 26 as an airgap'formed in it as shown. As shown in FIG. r example, the core may be positignedog the arrrr of the patient so that the artery 1% treated passes thr'dii'gh the airgap even though the core 26 and primary winding are positioned externally of the patient.
The primary winding 28 may be energized by an appropriate high frequency signal from a signal generator 30 of any suitable design. The frequency of the signal generated by the generator 30 may, for example, be in the range of from 25 lgihegzipmgahertz. Peak displacements of the order oil micrometer may beattained in the ro wrrfish'Efi paramet'rs areused.
A millivoltm gr g may be included in the circuit, and its peak reading may serve as a detection indicator to indicate the proper position of the external core 26 and primary winding 28 with respect to the internal moving element 14 and its secondary winding 22. That is, the external primary winding 28 and core 26 should be moved along the exterior of the ar tery 16 and turned as necessary as the element 14 is moved along its interior, with an optimum coupling relationship between the two being indicated by a maximum power flow through the meter 32. Furthermore, the meter 32 indicates the pc we lmggleansing process, and it also indicates any tendency for the core temperature to rise to a level at which it would injure the artery. Such a temperature rise may be offset by increasing the flow of solution introduced into the artery through the catheter 19 by means of a tube 21. The solution is' carried out of the artery to a filtering device through a second catheter 23 and tube 25. The catheter 23 extends through a second incision 27. This permits the fatty or other removed material to be studied and analyzed.
Although the element 14 is shown as directed and guided by the wire 18, the element could be configured so as to be inserted into the artery, and to move within the artery independently of any external guides, and by the arterial fluid itself. The movement of the element 14 could then be followed by the external coil 28 and core 26, as indicated by the deflection.
of the meter 32.
It will be appreciated, of course, that the embodiment illustrated in the drawing and described above is merely one aspect of the structural concept of the invention. For example, electrostrictive material such as barium titenate may be used, as will be described in conjunction with FIG. 5, and appropriate electrostatic fields produced by the voltage developed across an open secondary winding, rather than the current through a closed secondary winding as in the embodiment of FIG. 2. Moreover, a piezoelectg'c crystaLmay be used with plate contag ts, and with the secondary winding 66 nected to t e plate contacts and establishing control voltages across the crystal. The piezoelectric and electrostrictive rods do not require biasing.
in the embodiment of FIG. 4, the magnetostrictive element 140 is split, as shown, to have a U-shape defining a longitu- -dinal slot therein. The biasing permanent magnet 21a extends into the slot, out of contact with the element 140. The permanent magnet 21a is mounted on a disc 50 attached to the end of the push rod, or wire, 18. The element 140 may be attached to the disc 50 by compliant cement 20a which also forms the aforesaid damper. The secondary winding 22a is closed, as before, and is wound in a series-aiding relationship on the element 14a, as shown.
In the embodiment of FIG. 5 a piezoelggm'cflmlect fostrictive rod 14b is used and Lhe ends of the rod are metallizglby ele tric ggpla tsg and 54. The secondfiwiiiding 22b has ifs ends connected to the contacts 52 and 54 so as to provide an open circuit, with a voltage being applied across the contacts when the primary induces such a voltage in the secondary winding. A damper b is provided between the rod 14b and the head 50b of the push rod or wire 18. The secondary winding in the embodiment of FIG. 5, as in the previous embodiments may be old la t e c l nickel wire, or any other electrhzally conductive material which will not adversely affect the patient.
l. A medical instrument for removing deposits from the interior wall of an artery, or the like, of a subject, including: an element composed of magnetostrictive material configured to be received into the interior of the artery and can be moved therealong so as to establish mechanical vibrations within said artery with respect to an applied signal; an electrical winding mounted on said element to establish the aforesaid magnetostrictions therein upon the passage of an alternating current of ultrasonic frequency through said winding; a magnetic core of magnetizable material physically separated from said element and positioned externally of the subject; a primary winding mounted on said magnetic core and inductively coupled to the aforesaid electrical winding on said element; and means for causing an alternating current of ultrasonic frequency to flow in said primary winding.
2. The instrument defined in claim 1, and which includes a ring-shapedcore of magnetizable material supporting said primary winding and having an airgap therein.
3. The instrument defined in claim 1 and which includes a power source coupled to said primary winding for producing said alternating current in said primary winding, and an indicating meter coupled to said source to indicate the position of the aforesaid element with respect to said primary winding.
4. A medical instrument for removing deposits from the interior wall of an artery, or the like, including: an element composed of material configured to be received into the interior of the artery and to be moved therealong and to establish mechanical vibrations in response to an applied signal; and means coupled to said element for applying a signal thereto for establishing said vibrations therein as said element moves along the interior of the artery so as to cause the element to remove deposits from the interior wall of the artery, in which said element has an elongated rodlike configuration, and which includes electrical contacts mounted on the ends of said element, and which includes an electrical winding mounted on said element and having ends connected to said contacts to establish mechanical vibrations in said element upon the passage of an alternating current of ultrasonic frequency through said winding.
5. The medical instrument defined in claim 4, in which said element is composed of electrostrictive material.
6. The medical instrument defined in claim 4, in which said element is composed of piezoelectric material.
7. A medical instrument for removing deposits from the interior wall of an artery, or the like, including: an element composed of magnetostrictive material configured to be received into the interior of the artery and to be moved therealong and to establish mechanical vibrations in response to an applied signal; means coupled to said element for applying a signal thereto for establishing said vibrations therein as said element moves along the rntenor of the artery so as to cause the element to remove deposits from the interior wall of the artery, and which includes a biasing permanent magnet coupled to said element.
8. The medical instrument defined in claim 7, and which includes a damping member mounted on said element, and in which said biasing permanent magnet is mounted on said element and interposed between said clamping member and one end of said element.
9. The medical instrument defined in claim 7, and which includes a clamping member mounted on said element, and in which said biasing permanent magnet extends into a slot in said element.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3352303 *||Jul 28, 1965||Nov 14, 1967||Lawrence J Delaney||Method for blood clot lysis|
|US3433226 *||Jul 21, 1965||Mar 18, 1969||Aeroprojects Inc||Vibratory catheterization apparatus and method of using|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3830240 *||Jul 2, 1972||Aug 20, 1974||Blackstone Corp||Method and apparatus for disintegration of urinary calculi|
|US5095910 *||Apr 18, 1990||Mar 17, 1992||Advanced Technology Laboratories, Inc.||Ultrasonic imaging of biopsy needle|
|US5344395 *||Jan 24, 1992||Sep 6, 1994||Scimed Life Systems, Inc.||Apparatus for intravascular cavitation or delivery of low frequency mechanical energy|
|US5470307 *||Mar 16, 1994||Nov 28, 1995||Lindall; Arnold W.||Catheter system for controllably releasing a therapeutic agent at a remote tissue site|
|US5497043 *||Aug 6, 1993||Mar 5, 1996||The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland||Vibration reduction|
|US5880661 *||Apr 1, 1996||Mar 9, 1999||Emf Therapeutics, Inc.||Complex magnetic field generating device|
|US6007476 *||Oct 22, 1997||Dec 28, 1999||Emf Therapeutics, Inc.||Non-particle, non-photonic device and method for affecting angiogenesis|
|US6083149 *||Jul 8, 1998||Jul 4, 2000||Emf Therapeutics, Inc.||Magnetic field device and method for inhibiting angiogenesis and retarding growth rates of tumors in mammals|
|US6149577 *||Mar 18, 1999||Nov 21, 2000||Emf Therapeutics, Inc.||Apparatus and method for creating a substantially contained, finite magnetic field useful for relieving the symptoms pain and discomfort associated with degenerative diseases and disorders in mammals|
|US6221038 *||Nov 27, 1996||Apr 24, 2001||Pharmasonics, Inc.||Apparatus and methods for vibratory intraluminal therapy employing magnetostrictive transducers|
|US6320300 *||Sep 3, 1998||Nov 20, 2001||Lucent Technologies Inc.||Piezoelectric array devices|
|US6626940||Jun 15, 2001||Sep 30, 2003||Scimed Life Systems, Inc.||Medical device activation system|
|US6985770||Oct 26, 2001||Jan 10, 2006||Biosynergetics, Inc.||Apparatus for the controllable modification of compound concentration in a tube|
|US7616989||Nov 10, 2009||Biosynergetics, Inc.||Manufacturing methods for an apparatus for the controllable modification of compound concentration in a tube|
|US8295908 *||May 9, 2006||Oct 23, 2012||Eyoca Medical Ltd.||Device and method for opening vascular obstructions|
|US8317760||Nov 27, 2012||Biosynergetics, Inc.||Apparatus and methods for the controllable modification of compound concentration in a tube|
|US9014786||Jun 8, 2012||Apr 21, 2015||Eyoca Medical Ltd.||Device and method for opening vascular obstructions|
|US20020065493 *||Oct 26, 2001||May 30, 2002||Nyhart Eldon H.||Apparatus for the controllable modification of compound concentration in a tube|
|US20020115958 *||Oct 26, 2001||Aug 22, 2002||Nyhart Eldon H.||Manufacturing methods for an apparatus for the controllable modification of compound concentration in a tube|
|US20050025797 *||Jul 7, 2004||Feb 3, 2005||Xingwu Wang||Medical device with low magnetic susceptibility|
|US20050079132 *||Aug 9, 2004||Apr 14, 2005||Xingwu Wang||Medical device with low magnetic susceptibility|
|US20060173387 *||Dec 9, 2005||Aug 3, 2006||Douglas Hansmann||Externally enhanced ultrasonic therapy|
|US20080108935 *||Oct 31, 2007||May 8, 2008||Nyhart Eldon H Jr||Apparatus For The Controllable Modification Of Compound Concentration In A Tube|
|US20080293009 *||May 12, 2008||Nov 27, 2008||Winston Ronald H||Ultrasonic dental cleaner|
|US20080319373 *||Oct 31, 2007||Dec 25, 2008||Nyhart Eldon H Jr||Compound Delivery Tube|
|US20090209900 *||May 9, 2006||Aug 20, 2009||Eyoca Medical Ltd.||Device and method for opening vascular obstructions|
|WO1998034564A1 *||Feb 5, 1998||Aug 13, 1998||Intravascular Research Limited||Medical ultrasound apparatus|
|WO2002102456A1 *||May 30, 2002||Dec 27, 2002||Scimed Life Systems, Inc.||System for remotely actuating an implantable medical device and method of using the same|
|International Classification||A61M3/02, A61M5/00, A61B17/22, A61F2/02|
|Cooperative Classification||A61M3/0283, A61F2002/30668, A61B17/22012, A61B17/2202, A61F2250/0001, A61M5/00|
|European Classification||A61B17/22B2, A61B17/22B2D, A61M5/00|